medical MODERATE Updated 2026-04-08

Stryker Communications recalls Stryker CHROMOPHARE Softlit Ring Surgical Light System REF:

See all recalls from Stryker Communications →

Recalled Product

Stryker CHROMOPHARE Softlit Ring Surgical Light System REF: CH00000001

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Hazard / Issue

Surgical light assembly may not adequate support the weight of the ceiling cover.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI: 07613327296167; All Lots

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

Looking for a safe alternative?

Search Amazon for Stryker CHROMOPHARE Softlit Ring →

If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.

View official government recall

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